Laboratory Assistant II

Duration: 12 Months

The Laboratory Analyst II (Scientific ; Microbiology); (Temp Analyst) is dedicated to the Microbiology Laboratory. The role of the Laboratory Analyst II (Scientific ; Microbiology) will be that of various Microbial testing, data entry, EM Sample receipt, ordering and stocking supplies.

Job responsibilities:

The Laboratory Analyst II (Scientific; Microbiology) is part of the Quality Assurance Department at Ridgefield, NJ. This role is responsible for providing the day-to-day operation, Lab support and testing for the Micro team.

• The candidate must have basic quality control microbiology experience. Such as bioburden testing, membrane filtration, conductivity and total organic carbon is preferred.
• Basic knowledge of the pharmaceutical industry.
• Basic knowledge of compliance with all cGMP standards, safety and environmental regulations and company SOPs.
• Data entry of EM sampling results, LIMS, logbooks, and other miscellaneous lab data.
• Cohesive Micro player in the Micro department who is willing to assist or help a fellow analyst.

Analyst Qualifications:

• The Laboratory Analyst II (Scientific; Microbiology) is expected to act on and demonstrate the client’s LEAD competencies:
• Act for Change: Embrace change and innovation and initiate new and improved ways of working.
• Cooperate transversally: Collaborate effectively with peers, stakeholders and partners across the organization to positively impact business results.
• Develop People: Take responsibility for developing oneself and mentoring other Micro Personnel in anticipation of future business needs or to assist the micro department.

Job Requirements:

Physical Requirements include the capacity to lift and carry up to 20 pounds, kneel, reach, stretch, stocking supplies and to stand for at least 4 hours.

Requirements:

Education / Experience

• BA/BS in Microbiology/Biology with 1+ years’ experience in CGMP, pharma or lab environment is required.
• Practical experience in general microbiology laboratory techniques working.
• Working knowledge of cGMPs in pharmaceuticals/biological/aseptic/medical device manufacturing
• Excellent technical writing skills
• Ability to collaborate effectively with personnel and between departments.
• Problem-solving skills
• Strong communicator
• Works independently
• Working knowledge of Word, Excel and PowerPoint

HOURS: Consist of two possible shifts:

• Monday - Friday from 7:00 am to 3:30 pm, or

• Monday - Friday form 10:00 am to 6:30 pm

Some flex in the start and end times may be allowed; weekend work and overtime as required.